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Items: 1 to 20 of 562

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963234insertion1nstd209human GRCh38 chr10: 93,321,412-93,321,412 , GRCh37.p13 chr10: 95,081,169-95,081,169 MYOF
    nsv5959281insertion1nstd209human GRCh38 chr10: 93,478,834-93,478,834 , GRCh37.p13 chr10: 95,238,591-95,238,591 MYOF
    nsv5927453copy number variation1nstd209human GRCh38 chr10: 93,335,574-93,335,627 , GRCh37.p13 chr10: 95,095,331-95,095,384 MYOF
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5916956copy number variation1nstd209human GRCh38 chr10: 93,418,404-93,418,650 , GRCh37.p13 chr10: 95,178,161-95,178,407 MYOF
    nsv5914903copy number variation1nstd209human GRCh38 chr10: 93,335,781-93,335,859 , GRCh37.p13 chr10: 95,095,538-95,095,616 MYOF
    nsv5912947copy number variation1nstd209human GRCh38 chr10: 93,426,890-93,428,195 , GRCh37.p13 chr10: 95,186,647-95,187,952 MYOF
    nsv5911162copy number variation1nstd209human GRCh38 chr10: 93,307,342-93,307,670 , GRCh37.p13 chr10: 95,067,099-95,067,427 MYOF
    nsv5908592copy number variation1nstd209human GRCh38 chr10: 93,326,694-93,327,826 , GRCh37.p13 chr10: 95,086,451-95,087,583 MYOF
    nsv5866303copy number variation1nstd209human GRCh38 chr10: 93,326,749-93,327,798 , GRCh37.p13 chr10: 95,086,506-95,087,555 MYOF
    nsv5859227copy number variation1nstd209human GRCh38 chr10: 93,426,937-93,428,203 , GRCh37.p13 chr10: 95,186,694-95,187,960 MYOF
    nsv5712961mobile element insertion1nstd211human GRCh38 chr10: 93,357,797-93,357,797 , GRCh37.p13 chr10: 95,117,554-95,117,554 MYOF
    nsv5698930mobile element insertion1nstd211human GRCh38 chr10: 93,442,042-93,442,042 , GRCh37.p13 chr10: 95,201,799-95,201,799 MYOF
    nsv5628299insertion1nstd207human GRCh38 chr10: 93,478,832-93,478,832 , GRCh37.p13 chr10: 95,238,589-95,238,589 MYOF
    nsv5624636insertion1nstd207human GRCh38 chr10: 93,336,840-93,336,840 , GRCh37.p13 chr10: 95,096,597-95,096,597 MYOF
    nsv5604149copy number variation1nstd207human GRCh38 chr10: 93,335,574-93,335,627 , GRCh37.p13 chr10: 95,095,331-95,095,384 MYOF
    nsv5593142copy number variation1nstd207human GRCh38 chr10: 93,335,781-93,335,859 , GRCh37.p13 chr10: 95,095,538-95,095,616 MYOF
    nsv5585114copy number variation1nstd207human GRCh38 chr10: 93,326,694-93,327,826 , GRCh37.p13 chr10: 95,086,451-95,087,583 MYOF
    nsv5537990insertion1nstd206human GRCh38 chr10: 93,482,897-93,482,908 , GRCh37.p13 chr10: 95,242,654-95,242,665 MYOF
    nsv5493386copy number variation1nstd206human GRCh38 chr10: 93,415,523-93,415,607 , GRCh37.p13 chr10: 95,175,280-95,175,364 MYOF
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